c) Draw a mechanism for the formation of EtCH2COOH from the reaction of MeCOCH(Et)COOEt with NaOH in EtOH.

Q: Propose a mechanism for the reaction. Fill in the missing curved arrows in each step.

A: The given reaction is of dehydration of alcohol to alkene

Q: Draw a reasonable mechanism for the following reaction HO-S=0 HO OH OH

A: In this question, we will draw mechanism for each Reaction.

Q: Draw the major product(s) for reaction of methyl pentanoate with: (2) Me2CHCH2CH2OH, H3O*

A: Transesterification: The process of exchanging an alkyl group (R) of an ester with the alkyl group…

Q: Draw the product of attached reaction ?

A: In the reaction, following steps will take place. 1) The alkene given (not benzene) will take proton…

Q: Determine the mechanism of nucleophilic substitution for attached reaction anddraw the products,…

A: INTRODUCTION: SN1 reaction is a two step reaction in which first carbocation is formed that acts as…

Q: (a) Propose a mechanism for the following reaction: кон, н,о (b) What other product is formed?

A:

Q: H*, H2N

A: First Ketone will attack on H+ so that it can increase positive charge density on carbonyl Carbon…

Q: Br Br2 OH

A:

Q: NaO. + NaO Compound A

A: Attack of nucleophile to the carboxyl carbon of ester  Loss of leaving group leading to the…

Q: Select a possible mechanism for the reaction.

A:

Q: Propose a mechanism for the following reaction:

A: Acid-catalysed hydration reaction Carbocation intermediate Rearrangement possible 1,2- methyl Shift…

Q: Draw the mechanism for the following reaction: conc. H,SO4 Нeat (c)

A:

Q: OH

A:

Q: ден Please provide a mechanism for the following: а ден + Он Я ден H3C соон

A:

Q: MeH, Ме ОН N. Fill in the necessary reagents to complete the given reaction. ZI

A: Here we have to synthesize the following given compounds by using suitable reagents through…

Q: Ticls, k H2, Pdle CH3 Pooduch

A: In presence of TiCl3, McMurray coupling is occurred.  Followed by reduction of alkene .

Q: Draw

A: Water molecule react with H2O

Q: Draw the mechanism for the following reaction: CH Et- OH CH, Et

A: • Here, in this reaction 1-Chloro-2-methylcyclohexane is converted into Ethoxy-1-methylcyclohexane…

Q: Please draw a curved arrow mechanism for the posted aldol reaction: H,C CH3

A:

Q: Based on the image attached, explain the step-by-step mechanism reaction of nitration for methyl…

A: Nitration is carried out by concentrated HNO3 and H2SO4 mixture.  HNO3 + H2SO4 = NO2+ + H2O + H2SO4…

Q: :ÇI: CH3 + KOTBU H,C ČH3

A: Here, strong base/nucleophile is present, so there is a possibility of substitution as well as…

Q: Draw a stepwise detailed mechanism that illustrates how four organicproducts are formed in the…

A: Substitution reaction: When one functional group of a compound replaces the other functional group,…

Q: NaH

A: Aldol condensation : In presence of base when ketones or aldehyde reacts to another keto or aldehyde…

Q: 4. Provide the reagent(s) needed to complete the following reaction scheme. Provide the complete…

A:

Q: HN CH3B H,0 H* (cat)

A:

Q: c) Propose a mechanism for this reaction. BF3 Но HO.

A: BF3 , boron triflouride is lewis acid. So lone pair of oxygen of -OH group attack on it and…

Q: HO HO Draw the mechanism for the following reaction.

A:

Q: Draw the mechanism for thr reaction of an aldehyde or a ketone with hydride iron.

A: The carbonyl compounds undergo nucleophilic addition-elimination reaction.

Q: c). -O doilute HCI in CH3OH HO

A:

Q: Draw the complete mechanism for this reaction. p-CH3- CgH4– SO;H + H3C-OH

A: The organic conversion helps in the conversion of one organic compound into other compounds. This is…

Q: сн NaOCH,CH3 н CнCH2он heat

A:

Q: Draw a complete mechanism for the reaction below. HCI

A: Alkenes undergo addition reaction in the presence of hydrochloric acid, the addition follows…

Q: propose a mechanism

A: In the given reaction OH- attack at carbon of CO group and negative charges generates at Oxygen then…

Q: Draw a stepwise detailed reaction mechanism for the following reaction. HO + CgHsCHO H20 + `OH

A:

Q: Which is a correct mechanism step in the formation of an acetal?

A:

Q: Draw the mechanism for the following reaction. H.

A:

Q: Propose a mechanism for the α,β-elimination reaction.

A: A mechanism for the α,β-elimination reaction has to be given

Q: hv D. C.

A: This is an example of 1,3-sigmatropic carbon shift followed by electrocyclic ring opening.

Q: Draw the mechanism of how you can make cyclohexyl ethanoate from ethane

A: The details solution for this reaction is provided below in attach image.

Q: Can you explain the mechanism? Can you provide a shortcut?

A:

Q: Give a mechanism for the following reaction.

A: We have to predict the mechanism.

Q: H₂O H₂SO4 ?

A:

Q: HCI b.

A: First reaction involve allyl carbocation intermediate and second reaction is diels alder reaction

Q: CH3ONA in CH3OH ОН

A: The reaction starts with the attack of CH3O- to the C-O bond of ether to form a new ether bond and…

Q: Draw the mechanism for the reaction of cyclohexene with HCl.

A: The cyclohexene reacts with HCl via electrophilic addition.

Q: Draw the mechanism of the following reaction NaOH ONa HO +

A: This mechanism is an example of BAC2 mechanism. This is an example of hydrolysis of an ester.

Q: Draw the product of attached reaction ?

A: GIven,

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.